Regulatory Affairs Specialists

Regulatory Affairs Specialists

Full-Time 36000 - 60000 £ / year (est.) No working from home possible
LinkedIn

At a Glance

  • Tasks: Provide regulatory guidance and innovative strategies for medicinal product development.
  • Company: Scendea is a global leader in regulatory consulting, advancing healthcare innovation.
  • Benefits: Enjoy competitive salary, bonuses, private healthcare, and generous holiday allowances.
  • Other info: Opportunities for continuous learning and professional development in a supportive environment.
  • Why this job: Join a passionate team committed to problem-solving and making a positive societal impact.
  • Qualifications: Requires a life science degree, 8 years of drug development experience, and regulatory expertise.

The predicted salary is between 36000 - 60000 £ per year.

Are you looking to advance your career in regulatory affairs?At Scendea, we deliver market-leading scientific expertise and regulatory solutions to advance healthcare innovation worldwide. We are dedicated to streamlining medicinal product development, reducing time-to-market, and minimising costs for our biotech and pharmaceutical clients. If you are experienced in regulatory affairs and passionate about providing strategic and technical solutions to complex product development challenges, we’d love to hear from you.What’s involved?You will play a critical role in providing regulatory guidance and innovative strategies across a wide range of medicinal product development activities. This includes:Providing innovative drug development plans, data gap analyses and international regulatory strategies for complex products within the changing regulatory environment.Contributing to technical authorship and review of development regulatory documents including Regulatory Strategy Plans, Clinical and Drug Development Plans, Clinical Trial Applications, Pre-INDs, INDs, Scientific Advice and Meeting Briefing Documents, Orphan Drug and Paediatric plans/applications, Protocols, Investigator Brochures, IMPDs, CSRs, Marketing Authorisation Applications, New Drug Applications, Biologic License Applications, according to area of expertise.Representing clients in regulatory agency interactions and providing regulatory solutions to agency objections.Collaborating across jurisdictions and disciplines to deliver expert consulting services.What we are looking for:A high scientific calibre with a life science focused BSc (or equivalent), and a higher degree in a biomedical field or equivalent (e.g., a life science focused MSc or preferably a PhD).A minimum of 8 years of drug development experience.A minimum of experience with FDA, and/or MHRA/EMA, including negotiation. Regulatory experience may include time within a National Competent Authority.Direct experience preferred in providing strategic regulatory planning from early-stage development up to marketing authorisation, and a proven ability to define and deliver creative scientifically driven solutions to technical development and regulatory issues.Why Scendea?Scendea is an international product development and regulatory consulting group delivering market-leading scientific expertise & regulatory solutions, to advance healthcare innovation worldwide. We are passionate about delivering strategic and operational support to clients, with a strong commitment to problem-solving and redefining customer service. With a current team of over 50 staff based in the UK, Netherlands, Australia, and the US, Scendea is undergoing a period of significant growth, with the addition of new office locations and service lines to facilitate the delivery of expert and strategic global regulatory consulting services to our rapidly growing client base. We are equally committed to making a positive impact on society by managing our environmental impacts and contributing to a low-carbon economy. Our inclusive work culture values transparency, ethical collaboration with clients, and employee involvement in key decision-making processes, ensuring that our team is respected, supported, and engaged.As a Scendea EmployeePart of what makes Scendea successful is the highly motivated people who work for us and their enthusiasm for what we do and stand for. We recruit individuals whose passion, drive, integrity and customer orientation shines through. You are a motivated individual who can instil trust and confidence in our customer relationships whilst having a natural aptitude for getting the best out of people internally. You will inspire others through your commitment, motivation, expertise, professional manner and always placing the customer at the centre of everything you do.You will also receive;A competitive salary.Generous bonus program, which rewards success.Holiday plus public holidays, and discretionary additional days for birthday and work anniversary.Employer pension contribution.Provision of Private healthcare insurance.Access to Employee Assistance Programme.Employee Ownership Trust Scheme.A challenging and stimulating position for a dynamic and competent scientist, looking to contribute to a growing business and a rapidly expanding team.Coaching, mentoring and support of your continuous learning, and professional development within a highly recognised international team.Register your interest today!We are always looking for talented individuals to join our global team. If this sounds like the next step in your career, click “Apply” to register your interest.

Regulatory Affairs Specialists employer: LinkedIn

At Scendea, we pride ourselves on being an exceptional employer, offering a dynamic work environment that fosters innovation and collaboration in the field of regulatory affairs. Our inclusive culture prioritises employee growth through continuous learning opportunities, competitive salaries, and a generous benefits package, including private healthcare and a bonus programme. Join us in our mission to advance healthcare innovation while making a positive impact on society, all within a supportive and engaging team atmosphere.

LinkedIn

Contact Details:

LinkedIn Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Regulatory Affairs Specialists

Unlock Networking Opportunities

Dive into industry-specific events like pharmaceutical conferences and seminars, where you can meet hiring managers from companies like LinkedIn. These are goldmines for making connections and learning about job openings before they hit the mainstream job boards.

Join Relevant Professional Bodies

Get involved with organisations such as the Royal Pharmaceutical Society or your local pharmaceutical professionals' network. Being an active member can boost your credibility and may even lead to job referrals in top organisations like LinkedIn.

Leverage Internships for Full-time Roles

If you can, consider pursuing internships in the pharmaceutical industry, especially with companies like LinkedIn. These opportunities often pave the way for full-time positions and allow you to demonstrate your capabilities firsthand.

Tailor Your Approach

When you're applying for roles, don't rush it! Take the time to customise your applications for specific positions, showcasing relevant skills and experiences that align with what LinkedIn is looking for. A tailored application can really make you stand out!

We think you need these skills to ace Regulatory Affairs Specialists

Regulatory Knowledge
Drug Development Expertise
Technical Authoring
Clinical Trial Applications
FDA and EMA Regulations
Strategic Regulatory Planning
Data Gap Analysis

Some tips for your application 🫡

Showcase Your Relevant Experience:When applying for a role in the pharmaceutical industry, it's crucial to highlight any relevant experience you have. Whether that's internships, lab work, or even related coursework, make sure to weave this into your CV and cover letter. We want to see how your background aligns with the role you're applying for at LinkedIn!

Emphasise Your Understanding of Regulations:The pharmaceutical industry is heavily regulated, so it's important to indicate your familiarity with industry standards and regulations. In your cover letter, mention any training or certifications you've received that are relevant, or discuss projects where you’ve navigated compliance. This will show LinkedIn that you're not just a fit for the job but also a safety-conscious candidate!

Tailor Your CV to Be Result-Driven:Craft your CV to highlight quantifiable achievements, especially if you have previous roles in pharmaceuticals or related fields. Use metrics to demonstrate your impact, such as improved processing times or successful project completions while working on trials. This analytical approach will resonate well with hiring managers at LinkedIn!

Convey Your Passion for the Industry:In your cover letter, express why you are passionate about working in the pharmaceutical sector. Whether it’s your desire to contribute to groundbreaking drug research or improve patient outcomes, let it shine through! At LinkedIn, we value candidates who are truly enthusiastic about their work—you might just stand out from the crowd.

How to prepare for a job interview at LinkedIn

Understand the Science

Make sure you brush up on key pharmaceutical concepts and recent developments in the industry. You might get asked some technical questions during the interview at LinkedIn that show your grasp of drug development processes or regulatory requirements, so be ready to discuss them clearly.

Showcase Relevant Experience

If you have any hands-on experience or internships in a laboratory setting, be sure to highlight these in your responses. Think about the projects you worked on, the methodologies you used, and the impact you made. It's all about telling a story that connects your background to the role you're applying for.

Know Their Products

Take some time to familiarise yourself with LinkedIn’s product range and recent breakthroughs. Understanding their portfolio not only shows your enthusiasm for the role but also allows you to ask insightful questions that demonstrate your interest in actively contributing to their projects.

Be Ready for Regulatory Scenarios

In a full-time pharmaceutical role, understanding the regulatory landscape is crucial. Prepare for situational questions that may test your problem-solving skills concerning compliance and safety standards. You could be asked how you'd handle a hypothetical issue regarding a drug’s market release, so think through your approach.